Andrea Mayrhofer
University of Hertfordshire
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Featured researches published by Andrea Mayrhofer.
Dementia | 2015
Andrea Mayrhofer; Claire Goodman; Cheryl Holman
This discussion paper considers the currently evolving roles of dementia champions and describes an initiative designed to support their activities. The aim of this initiative was to establish a county-wide group that has a shared group identity and sufficient critical mass that is able to identify and implement dementia training and development needs for the health and social care workforce. The approach used to achieve this aim was a Dementia Champion Community of Practice Project, which involved dementia leads in various NHS Trusts. Whilst this approach might be effective at practitioner level, the Dementia Champion Community of Practice Project experience suggests that if such initiatives are to be sustainable they need to be strategically placed within networks that can bring together service providers, educators and commissioners.
Aging & Mental Health | 2017
Andrea Mayrhofer; Elspeth Mathie; Jane McKeown; Frances Bunn; Claire Goodman
ABSTRACT Background: Literature agrees that post-diagnostic services for people living with young onset dementia (YOD) need to be age-appropriate, but there is insufficient evidence of ‘what works’ to inform service design and delivery. Objective: To provide an evidence base of age-appropriate services and to review the perceived effectiveness of current interventions. Methods: We undertook a systematic review including all types of research relating to interventions for YOD. We searched PubMed, CINHAL Plus, SCOPUS, EBSCO Host EJS, Social Care Online and Google Scholar, hand-searched journals and carried out lateral searches (July–October 2016). Included papers were synthesised qualitatively. Primary studies were critically appraised. Results: Twenty articles (peer-reviewed [n = 10], descriptive accounts [n = 10]) discussing 195 participants (persons diagnosed with YOD [n = 94], caregivers [n = 91] and other [n = 10]) were identified for inclusion. Services enabled people with YOD to remain living at home for longer. However, service continuity was compromised by short-term project-based commissioning and ad-hoc service delivery. Conclusion: The evidence on the experience of living with YOD is not matched by research and the innovation needed to mitigate the impact of YOD. The inclusion of people with YOD and their caregivers in service design is critical when planning support in order to delay institutional care
The Journal of Mental Health Training, Education and Practice | 2016
Andrea Mayrhofer; Claire Goodman
Purpose – People with dementia require care at home, in care homes and in hospitals, which has implications for the current and future workforce in health and social care. To inform regional workforce development planning in dementia care, Health Education East of England commissioned an organisational audit of current dementia training at NHS Trusts and in social care across Hertfordshire and Bedfordshire. The paper aims to discuss this issue. Design/methodology/approach – Qualitative methods and non-probability purposive sampling were used for recruitment and data collection. The audit included NHS Trusts, local authorities, clinical commissioning groups, and health and social care organisations involved in commissioning and providing dementia education and training in the two counties. Findings – Whilst there was considerable investment in dementia awareness training, learning was not targeted, assessed or structured to ensure on-going professional development. Practical implications – This has implica...
Dementia | 2016
Andrea Mayrhofer; Claire Goodman; Nigel Smeeton
Background The conceptualisation and development of the role of Dementia Champions in clinical practice is ongoing, and dementia specific training has a significant impact on the scope of the role. Aim This survey aimed to elicit Dementia Champions’ views on their role and associated training needs. Methods Data were collected via an online survey. Findings Of 188, 34 Dementia Champions (response rate 18%) participated. Most perceived dementia awareness training as useful, but limited. Areas suggested for further development were context specific skills training, education programmes that were formally recognised, and clarification around the expectations of the role. Conclusion Expectations of ‘champion roles’ in dementia need to be re-visited, specifically in relation to the remit of the role and the level of education, preparation and support required for Dementia Champions to become change agents in dementia care.
International Journal of Geriatric Psychiatry | 2018
Michael Woodward; Antony Arthur; Nicole Darlington; Stefanie Buckner; Anne Killett; John Thurman; Marina Buswell; Louise Lafortune; Elspeth Mathie; Andrea Mayrhofer; Claire Goodman
The dementia‐friendly community (DFC) initiative was set up to enable people living with dementia to remain active, engaged, and valued members of society. Dementia prevalence varies nationally and is strongly associated with the age and sex distribution of the population and level of social deprivation. As part of a wider project to evaluate DFCs, we examined whether there is a relationship between provision of DFCs and epidemiological need.
Dementia | 2018
Andrea Mayrhofer; Elspeth Mathie; Jane McKeown; Claire Goodman; Lisa Irvine; Natalie Hall; Michael Walker
Whilst the support requirements of people diagnosed with young onset dementia are well-documented, less is known about what needs to be in place to provide age-appropriate care. To understand priorities for service planning and commissioning and to inform the design of a future study of community-based service delivery models, we held two rounds of discussions with four groups of people affected by young onset dementia (n = 31) and interviewed memory services (n = 3) and non-profit service providers (n = 7) in two sites in England. Discussions confirmed published evidence on support requirements, but also reframed priorities for support and suggested new approaches to dementia care at the community level. This paper argues that involving people with young onset dementia in the assessment of research findings in terms of what is important to them, and inviting suggestions for solutions, provides a way for co-designing services that address the challenges of accessing support for people affected by young onset dementia.
Age and Ageing | 2018
Adam Gordon; Claire Goodman; Sue Davies; Tom Dening; Heather Gage; Julienne Meyer; Justine Schneider; Brian G. Bell; Jake Jordan; Finbarr C. Martin; Steve Iliffe; Clive Bowman; John Gladman; Christina R. Victor; Andrea Mayrhofer; Melanie Handley; Maria Zubair
Abstract Introduction care home residents have high healthcare needs not fully met by prevailing healthcare models. This study explored how healthcare configuration influences resource use. Methods a realist evaluation using qualitative and quantitative data from case studies of three UK health and social care economies selected for differing patterns of healthcare delivery to care homes. Four homes per area (12 in total) were recruited. A total of 239 residents were followed for 12 months to record resource-use. Overall, 181 participants completed 116 interviews and 13 focus groups including residents, relatives, care home staff, community nurses, allied health professionals and General Practitioners. Results context-mechanism-outcome configurations were identified explaining what supported effective working between healthcare services and care home staff: (i) investment in care home-specific work that legitimises and values work with care homes; (ii) relational working which over time builds trust between practitioners; (iii) care which ‘wraps around’ care homes; and (iv) access to specialist care for older people with dementia. Resource use was similar between sites despite differing approaches to healthcare. There was greater utilisation of GP resource where this was specifically commissioned but no difference in costs between sites. Conclusion activities generating opportunities and an interest in healthcare and care home staff working together are integral to optimal healthcare provision in care homes. Outcomes are likely to be better where: focus and activities legitimise ongoing contact between healthcare staff and care homes at an institutional level; link with a wider system of healthcare; and provide access to dementia-specific expertise.
BMC Palliative Care | 2015
Claire Goodman; Katherine Froggatt; Sarah Amador; Elspeth Mathie; Andrea Mayrhofer
BMC Palliative Care | 2016
Andrea Mayrhofer; Claire Goodman; Nigel Smeeton; Melanie Handley; Sarah Amador; Sue Davies
Health Services and Delivery Research | 2017
Claire Goodman; Sue Davies; Adam Gordon; Tom Dening; Heather Gage; Julienne Meyer; Justine Schneider; Brian G. Bell; Jake Jordan; Finbarr C. Martin; Steve Iliffe; Clive Bowman; John Gladman; Christina R. Victor; Andrea Mayrhofer; Melanie Handley; Maria Zubair